| Approved symbol | CHM |
|---|---|
| Approved name | CHM Rab escort protein |
| HGCN ID | HGNC:1940 |
| Previous symbols | TCD, DXS540 |
| Inheritance | |
| OMIM | 300390 |
| Chromosome | Xq21.2 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Congenital stationary nightblindness NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB |
